| Project/Area Number |
23790991
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| Research Category |
Grant-in-Aid for Young Scientists (B)
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| Allocation Type | Multi-year Fund |
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| Research Field |
Neurology
|
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| Research Institution | Okayama University |
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Principal Investigator |
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| Project Period (FY) |
2011 – 2012
|
| Project Status |
Completed (Fiscal Year 2012)
|
| Budget Amount *help |
¥2,600,000 (Direct Cost: ¥2,000,000、Indirect Cost: ¥600,000)
Fiscal Year 2012: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2011: ¥1,560,000 (Direct Cost: ¥1,200,000、Indirect Cost: ¥360,000)
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| Keywords | 慢性期脳梗塞 / 再生治療 / 軸索伸長関連因子 / ゼラチン多孔体 / 軸索伸長阻害因子 / 軸索伸長促進因子 / 脳梗塞 / 血管新生 / ペリサイト |
|---|
| Research Abstract |
Changes in expression of neurorepair and neuroregenerative factors, which were important for the regeneration therapy of the chronic stage cerebral ischemia, were examined after transient rat cerebral ischemia. Immunohistochemistry and western blot analyses indicated that axonal growth inhibiting protein expression of neurocan, Sema3A, Nogo-R, and promoting protein expression of deleted in colorectal cancer was increased with edaravone, which was one of the free radical scavenger. The present study demonstrates that these protein factors ameliorated such damage inbrain repair after ischemia.
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